SHMARQL

tetralogy of Fallot

<http://www.wikidata.org/entity/Q1126831>

congenital heart defect, whose symptoms include episodes of bluish skin color, whose embryology includes anteriosuperior displacement of the infundibular (aorticopulmonary) septum
tetralogy of Fallot
rdfs:label
"tetralogy of Fallot"@en
skos:altLabel
"Fallot tetralogy"@en
"TETRALOGY OF FALLOT"@en
"TETRALOGY OF FALLOT; TOF"@en
"TOF"@en
"Ventricular septal defect with pulmonary stenosis or atresia, dextraposition of aorta, and hypertrophy of right ventricle"@en
schema:description
"congenital heart defect, whose symptoms include episodes of bluish skin color, whose embryology includes anteriosuperior displacement of the infundibular (aorticopulmonary) septum"@en
schema:dateModified "2026-10-24T00:08:27+00:00"^^xsd:dateTime
schema:version 2560162829
wikibase:identifiers 39
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p:direct-normalized/P244 <http://id.loc.gov/authorities/names/sh85134202>
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p:direct-normalized/P508 <http://purl.org/bncf/tid/27155>
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<http://id.nlm.nih.gov/mesh/C14.280.400.849>
<http://id.nlm.nih.gov/mesh/C16.131.240.400.849>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:6419>
wdt:P10565 "464656"
"577234"
wdt:P11143 "Tetralogy of Fallot"
wdt:P11430 "DI-02362"
wdt:P12385 "tetralogia-de-fallot"
wdt:P1245 "1383669"
wdt:P1296 "0025909"
wdt:P1325 <http://www.nanbyou.or.jp/entry/4741>
wdt:P13591 "concept/3b8cdc18-0bf6-4a28-8953-fe5f8d0f39e2"
wdt:P138 Arthur Fallot
wdt:P1417 "science/tetralogy-of-Fallot"
wdt:P14541 "2MJ4Iy"
wdt:P1461 "fallots-tetralogy"
wdt:P14914 "D03303"
wdt:P1550 "3303"
wdt:P1692 "745.2"
wdt:P1748 "C84505"
wdt:P18 <http://commons.wikimedia.org/wiki/Special:FilePath/Tetralogy%20of%20Fallot.svg>
wdt:P1889 teratology
wdt:P1995 pediatrics
cardiac surgery
wdt:P2176 alprostadil
wdt:P2293 GDF1
NKX2-5
FLT4
GATA6
GJA5
KDR
TBX1
NRP1
CITED2
ZFPM2
NKX2-6
GATA5
JAG1
GATA4
GPC5
wdt:P2347 "39151"
wdt:P244 "sh85134202"
wdt:P268 "12336440c"
wdt:P279 trilogy of Fallot
cyanotic heart defect
wdt:P2841 congenital onset
neonatal onset
wdt:P2888 <http://identifiers.org/doid/DOID:6419>
<http://purl.obolibrary.org/obo/DOID_6419>
<http://purl.obolibrary.org/obo/HP_0001636>
<http://www.orpha.net/ORDO/Orphanet_3303>
wdt:P2892 "C0039685"
wdt:P31 type of disease
designated intractable/rare disease
rare disease
wdt:P3417 "Tetralogy-of-Fallot"
wdt:P3471 "1366"
wdt:P373 "Tetralogy of Fallot"
wdt:P3827 "tetralogy-of-fallot"
wdt:P3841 "HP:0001636"
wdt:P4229 "Q21.3"
wdt:P4233 "tetralogy-of-fallot"
wdt:P4317 "2245"
wdt:P486 "D013771"
wdt:P492 "187500"
wdt:P5008 WikiProject Medicine
wdt:P508 "27155"
wdt:P5270 "MONDO_0008542"
wdt:P557 "4660"
wdt:P604 "001567"
wdt:P6366 "2908714464"
wdt:P6532 Broad forehead
tetralogy of Fallot
intrauterine growth restriction
preauricular fistulae, congenital
exophthalmos
dolichocephaly
brachydactyly
cryptorchidism
wdt:P665 "H00549"
wdt:P672 "C14.240.400.849"
"C14.280.400.849"
"C16.131.240.400.849"
wdt:P673 "2035949"
wdt:P699 "DOID:6419"
wdt:P7329 "LA88.2"
wdt:P7807 "90973426"
wdt:P8189 "987007531882305171"
wdt:P8313 "Steno-Fallots_tetralogi"
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